PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
23566952-4	2013	The results showed that SFN inhibited TCDD-induced CYP1A1 activity in H4IIE cells by directly inhibiting CYP1A1 activity, probably through binding to aryl hydrocarbon receptor and/or CYP1A1 revealed by molecular docking.	sulforaphane	24-27	aryl hydrocarbon receptor	Rattus norvegicus	150-175	
22643862-2	2012	It is demonstrated in this paper that the isothiocyanates R,S-sulforaphane and erucin are non-competitive antagonists of the aryl hydrocarbon (Ah) receptor.	sulforaphane	58-74	aryl hydrocarbon receptor	Rattus norvegicus	125-155	
22643862-5	2012	In further studies, it was demonstrated that R,S-sulforaphane could both prevent the interaction of and displace already bound benzo[a]pyrene from the Ah receptor, but no concentration dependency was observed with respect to the isothiocyanate.	sulforaphane	45-61	aryl hydrocarbon receptor	Rattus norvegicus	151-162	
22643862-7	2012	Of the two isomers of R,S-sulforaphane, the naturally occurring R-isomer was more effective than the S-isomer in antagonizing the activation of the Ah receptor by benzo[a]pyrene.	sulforaphane	22-38	aryl hydrocarbon receptor	Rattus norvegicus	148-159